Abstract Claims Description Full Text

Claims

The invention claimed is:

1. A solid orally administrable pharmaceutical dosage form comprising:

a first portion containing a therapeutically effective amount of a histamine H₂ -receptor antagonist; and

a second portion immediately adjacent the first portion without an intervening barrier disposed between the first portion and the second portion, the second portion containing a therapeutically effective amount of an antacid.

2. The dosage form of claim 1, wherein the histamine H₂ -receptor antagonist is selected from compounds represented by the formula: ##STR2##

wherein R represents a hydrogen atom or a lower alkyl group; R₁ represents an amino group, a mono- or di-lower alkyl amino group, an aryl amino group or an aralkyl amino group; R₂ represents a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group; Y represents a sulfur atom or a methylene group; m and n each represent an integer of 1-3.

3. The dosage form of claim 1, wherein the histamine H₂ -receptor antagonist is selected from cimetidine, ranitidine and famotidine.

4. The dosage form of claim 1, wherein the antacid is selected from aluminum carbonate, aluminum hydroxide, aluminum phosphate, aluminum hydroxy carbonate, dihydroxy aluminum sodium carbonate, aluminum magnesium glycinate, dihydroxy aluminum aminoacetate, dihydroxy aluminum aminoacetic acid, bismuth aluminate, bismuth carbonate, bismuth subcarbonate, bismuth subgallate, bismuth subnitrate, calcium carbonate, calcium phosphate, hydrated magnesium aluminate, activated sulfate, magnesium aluminate, magnesium aluminosilicates, magnesium carbonate, magnesium glycinate, magnesium hydroxide, magnesium oxide, magnesium trisilicate, sodium bicarbonate and combinations of two or more of these antacids.

5. A solid orally administrable pharmaceutical dosage form comprising:

a first layer containing a therapeutically effective amount of a histamine H₂ -receptor antagonist; and

a second layer immediately adjacent the first layer without an intervening barrier layer disposed between the first layer and the second layer, the second layer containing a therapeutically effective amount of an antacid.

6. The dosage form of claim 5, wherein the histamine H₂ -receptor antagonist is selected from compounds represented by the formula: ##STR3##

wherein R represents a hydrogen atom or a lower alkyl group; R₁ represents an amino group, a mono- or di-lower alkyl amino group, an aryl amino group or an aralkyl amino group; R₂ represents a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group; Y represents a sulfur atom or a methylene group; m and n each represent an integer of 1-3.

7. The dosage form of claim 5, wherein the histamine H₂ -receptor antagonist is selected from cimetidine, ranitidine and famotidine.

8. The dosage form of claim 5, wherein the antacid is selected from aluminum carbonate, aluminum hydroxide, aluminum phosphate, aluminum hydroxy carbonate, dihydroxy aluminum sodium carbonate, aluminum magnesium glycinate, dihydroxy aluminum aminoacetate, dihydroxy aluminum aminoacetic acid, bismuth aluminate, bismuth carbonate, bismuth subcarbonate, bismuth subgallate, bismuth subnitrate, calcium carbonate, calcium phosphate, hydrated magnesium aluminate, activated sulfate, magnesium aluminate, magnesium aluminosilicates, magnesium carbonate, magnesium glycinate, magnesium hydroxide, magnesium oxide, magnesium trisilicate, sodium bicarbonate and combinations of two or more of these antacids.

9. The dosage form of claim 5, wherein the antacid in the second layer is selected from magnesium hydroxide, calcium carbonate, and a combination of both magnesium hydroxide and calcium carbonate.

10. The dosage form of claim 5, wherein the antacid in the second layer is selected from magnesium hydroxide, calcium carbonate, and a combination of both magnesium hydroxide and calcium carbonate, and wherein the histamine H₂ -receptor antagonist is famotidine.

11. The dosage form of claim 5, further comprising a third layer containing a second antacid.

12. The dosage form of claim 11, wherein the histamine H₂ -receptor antagonist is famotidine, the antacid in the second layer is one of magnesium hydroxide and calcium carbonate, and the antacid in the third layer is the other of magnesium hydroxide and calcium carbonate.

13. A process of preparing a multiple layer tablet containing a histamine H₂ -receptor antagonist and an antacid, comprising:

blending a first active ingredient selected from the antacid and the histamine H₂ -receptor antagonist with suitable excipients and/or adjuvants to form a first mixture;

compressing the first mixture to form a first layer of the tablet;

blending the other of the antacid and histamine H₂ -receptor antagonist with excipients and/or adjuvants to form a second mixture; and

compressing the second mixture directly on the first layer to form a second layer without any intervening barrier layer between the first layer and second layer.

14. The process of claim 13, wherein the histamine H₂ -receptor antagonist is selected from compounds represented by the formula: ##STR4##

wherein R represents a hydrogen atom or a lower alkyl group; R₁ represents an amino group, a mono- or di-lower alkyl amino group, an aryl amino group or an aralkyl amino group; R₂ represents a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group; Y represents a sulfur atom or a methylene group; m and n each represent an integer of 1-3.

15. The process of claim 13, wherein the histamine H₂ -receptor antagonist is selected from cimetidine, ranitidine and famotidine.

16. The process of claim 13, wherein the antacid is selected from aluminum carbonate, aluminum hydroxide, aluminum phosphate, aluminum hydroxy carbonate, dihydroxy aluminum sodium carbonate, aluminum magnesium glycinate, dihydroxy aluminum aminoacetate, dihydroxy aluminum aminoacetic acid, bismuth aluminate, bismuth carbonate, bismuth subcarbonate, bismuth subgallate, bismuth subnitrate, calcium carbonate, calcium phosphate, hydrated magnesium aluminate, activated sulfate, magnesium aluminate, magnesium aluminosilicates, magnesium carbonate, magnesium glycinate, magnesium hydroxide, magnesium oxide, magnesium trisilicate, sodium bicarbonate and combinations of two or more of these antacids.

17. The process of claim 13, wherein the antacid in the second layer is selected from magnesium hydroxide, calcium carbonate, and a combination of both magnesium hydroxide and calcium carbonate.

18. The process of claim 13, wherein the antacid in the second layer is selected from magnesium hydroxide, calcium carbonate, and a combination of both magnesium hydroxide and calcium carbonate, and wherein the histamine H₂ -receptor antagonist is famotidine.

19. The process of claim 13, further comprising a third layer containing a second antacid.

20. The process of claim 19, wherein the histamine H₂ -receptor antagonist is famotidine, the antacid in the second layer is one of magnesium hydroxide and calcium carbonate, and the antacid in the third layer is the other of magnesium hydroxide and calcium carbonate.